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Lens Cutter Forceps

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
LENS CUTTER FORCEPS FDA UDI
Generic Name
Intraocular lens removal scissors, conventional-hinge, reusable FDA UDI
Device Name
INTRAOCULAR LENS CUTTER FORCEPS MCKOOL STYLE FLAT TITANIUM HANDLE FDA UDI
Model / Reference
13-5390 FDA UDI
Description
INTRAOCULAR LENS CUTTER FORCEPS MCKOOL STYLE FLAT TITANIUM HANDLE FDA UDI

Identifiers

Catalog Number
13-5390 FDA UDI
Primary DI / UDI-DI
00192896095878 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular lens removal scissors, conventional-hinge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 4.5 Inch FDA UDI

Category: Intraocular lens removal scissors, conventional-hinge, reusable

Lens Cutter Forceps by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular lens removal scissors, conventional-hinge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 4ddab3e7-4542-4b4c-9cdd-181846fb5dce 36 fields · synced May 30, 2026